Ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin and synthesis thereof, ternary resin and preparation thereof, and composite material and preparation thereof

An ethynyl phenyl, base propargyl ether technology, applied in the fields of polymer chemistry, polymer physics and polymer material modification, can solve the problems of low mechanical properties and poor thermal stability of composite materials

Active Publication Date: 2018-11-06
EAST CHINA UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0012] The technical problem to be solved by the present invention is to overcome the technical problems that the thermal stability of the silicon-containing aryl propargyl ether resin in the prior art is not strong, and the mechanical properties of t

Method used

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  • Ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin and synthesis thereof, ternary resin and preparation thereof, and composite material and preparation thereof
  • Ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin and synthesis thereof, ternary resin and preparation thereof, and composite material and preparation thereof
  • Ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin and synthesis thereof, ternary resin and preparation thereof, and composite material and preparation thereof

Examples

Experimental program
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Effect test

Embodiment 3

[0085] In Example 3 and Example 4, the cyanate raw material was purchased from Yangzhou Tianqi New Materials Co., Ltd., bisphenol A cyanate monomer was selected, the product model was CE01MO, and bisphenol E cyanate monomer was selected. The product model is CE09MO.

[0086] In the data testing part, the structure of the resin is tested by a hydrogen nuclear magnetic resonance instrument. The curing reaction temperature of resin can be tested by differential scanning calorimeter (DSC), and the initial temperature of curing reaction (T i ), and curing reaction peak temperature (T p ), curing reaction end temperature (T f ) and the exothermic enthalpy of the curing reaction (ΔH). The curing process of the resin can be determined by referring to the results of the resin DSC test. The thermal stability of the thermally cured resin can be tested in a nitrogen atmosphere with a thermogravimetric analyzer (TGA), and the 5% thermal weight loss temperature (T d5 ) and 800℃ residua...

Embodiment 1

[0092] Synthesis of ethynylphenyl-terminated silicon-containing bisphenol A propargyl ether resin:

[0093] The first step: the 500mL four-neck flask 1 equipped with mechanical stirring, reflux condenser, thermometer, constant pressure funnel and nitrogen inlet and outlet is vacuum pumped and roasted three times, feeds nitrogen, and takes by weighing 6.6g (0.275mol) of magnesium powder and 50mL Add THF into a four-necked flask, slowly add a solution of 28.6g (0.263mol) bromoethane and 50mL THF dropwise, control the temperature below 25°C, heat to 45°C after dropping, and keep warm for 2h to obtain ethyl bromide Magnesium Grignard reagent, cooled to room temperature with an ice-water bath; weigh 38.0g (0.125mol) of bisphenol A dipropargyl ether and dissolve it in 50mL of THF, slowly drop the solution into the reaction flask, control the temperature below 25°C, After dropping, heat to 65°C, reflux for 2h, and cool to room temperature; weigh 32.27g (0.25mol) of dimethyldichlorosi...

Embodiment 2

[0108] Preparation of ethynylphenyl-terminated silicon-containing bisphenol A propargyl ether resin by butyllithium method:

[0109] Step 1: Vacuum bake a 500mL four-neck flask equipped with mechanical stirring, reflux condenser, thermometer, constant pressure funnel and nitrogen gas inlet and outlet three times, and then blow nitrogen gas into it. Weigh 30.42g of bisphenol A dipropargyl ether and 100mL of THF into the four-neck flask I, stir evenly; use a liquid nitrogen / ethanol bath to cool down to -10°C, extract 80mL of 2.5M n-butyllithium solution, and pass Slowly add dropwise through a constant pressure dropping funnel; after the dropwise addition, warm up to room temperature and react for 2 hours; cool down to -10°C with a liquid nitrogen / ethanol bath; weigh 25.8g of dimethyldichlorosilane and dissolve it in 100mLTHF, The dropping funnel was slowly added dropwise to the reaction flask I; the temperature was raised to room temperature for 0.5h; the intermediate product wa...

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Abstract

The invention discloses ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin and synthesis thereof, ternary resin and preparation thereof, and a composite material and preparation thereof. The structural formula of the silicon-containing aryl propargyl ether resin is shown in a formula II, and the polymerization degree n is equal to 2 to 3. The formed silicon-containing aryl propargyl ether resin with a novel terminal group structure improves the heat stability, and improves the mechanical property of ethynyl phenyl-terminated silicon-containing aryl propargyl ether modifiedresin through blending with cyanate ester and benzoxazine, thereby providing the ethynyl phenyl-terminated silicon-containing aryl propargyl ether resin with excellent mechanical property and good heat resistance, and is applied to preparation of carbon fiber reinforced composite materials.

Description

technical field [0001] The invention relates to the technical fields of polymer chemistry, polymer physics and polymer material modification, in particular to a silicon-containing aryl propargyl ether resin terminated by ethynyl phenyl group and its synthesis, ternary resin and its preparation and compounding Materials and their preparation. Background technique [0002] The carrier speed of aerospace and transportation is getting faster and faster, and the development of thin and light electronic products requires materials with high heat resistance, light weight and good strength. The development of high-tech polymer materials can meet the needs of aerospace and electronic information for new materials. [0003] In order to overcome the decline of the physical-mechanical properties of composite materials caused by the water absorption (~5%) of epoxy resin and bismaleimide resin in a hot and humid environment, U.S. Patent (US4 885 403, 1989) discloses a Preparation of bis...

Claims

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Application Information

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IPC IPC(8): C07F7/08C08L79/04C08K5/5419C08J5/04
CPCC07F7/0827C08J5/042C08J2379/04C08J2479/04C08L79/04C08L2205/025C08K5/5419
Inventor 袁荞龙黄发荣郑嘉栋
Owner EAST CHINA UNIV OF SCI & TECH
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